The choice of surgical approach for thalamic tumors

SMRČKA, Martin, Eva BRICHTOVÁ a Vilém JURÁŇ. The choice of surgical approach for thalamic tumors. In 24th Congress of the European Society for Pediatric Neurosurgery (ESPN). 2014. ISSN 0256-7040. Dostupné z: https://dx.doi.org/10.1007/s00381-014-2389-4.

Základní údaje

• Originální název: The choice of surgical approach for thalamic tumors
• Autoři: SMRČKA, Martin (203 Česká republika, garant, domácí), Eva BRICHTOVÁ (203 Česká republika, domácí) a Vilém JURÁŇ (203 Česká republika, domácí).
• Vydání: 24th Congress of the European Society for Pediatric Neurosurgery (ESPN), 2014.

Další údaje

• Originální jazyk: angličtina
• Typ výsledku: Konferenční abstrakt
• Obor: 30200 3.2 Clinical medicine
• Stát vydavatele: Spojené státy
• Utajení: není předmětem státního či obchodního tajemství
• Impakt faktor: Impact factor: 1.114
• Kód RIV: RIV/00216224:14110/14:00075577
• Organizační jednotka: Lékařská fakulta
• ISSN: 0256-7040
• Doi: http://dx.doi.org/10.1007/s00381-014-2389-4
• Klíčová slova anglicky: Thalamic tumors
• Štítky: EL OK

Anotace

Introduction: Thalamic tumors are relatively rare tumors growing in a highly functional part of brain. They are more frequent in pediatric population. Their surgery is challenging and a high morbidity is possible. Relatively benign nature of many of these tumors means that an attempt for radical resection should frequently be performed. The approach has to be very carefully planned, sometimes with the help of modern diagnostic methods like DTI. The location and projection of the tumor in the thalamus playes an important role in choosing the approach. The pitfals of these approaches are presented Material: We have studied a group of 12 pediatric patients with thalamic tumors treated from 2005 - 2012. There were 9 males and 3 females, age ranged from 1-18 years (mean 11 years). Transcortical approach was used 4x, transcallosal 4x, transsylvian 2x and supracerebellar infratentorial 2x. Results: Gross total resection was achieved in 5 cases, subtotal in 4 and partial in 3. There were 9 pilocytic astrocytomas, one subependymal giant cell astrocytoma, one diffuse astrocytoma G II and one glioblastoma. All patients are still alive with the mean follow-up 5 years. There was no permanent morbidity in this group. Conclusion: Thalamic tumors might be safely radically resected if correct approach is used. The choice of approach is based in the projection of the tumor. Smaller tumors which are not close to the thalamic surface might be followed or biopsied if there is a likelihood of its malignIt nature. Oncological treatment should be reserved for malignant tumors.